phenylalanine and Fukuhara Disease

phenylalanine has been researched along with Fukuhara Disease in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Filosto, M; Galli, R; Mancuso, M; Murri, L; Pizzanelli, C; Siciliano, G	1
Alfonzo, JD; Fredrick, K; Ibba, M; Ling, J; Qin, D; Roy, H; Rubio, MA	1

Other Studies

2 other study(ies) available for phenylalanine and Fukuhara Disease

Article	Year
Antimyoclonic effect of levetiracetam in MERRF syndrome. Journal of the neurological sciences, 2006, Apr-15, Volume: 243, Issue:1-2 Topics: Activities of Daily Living; Anticonvulsants; Atrophy; Brain; Drug Therapy, Combination; Female; Genetic Predisposition to Disease; Humans; Levetiracetam; MERRF Syndrome; Middle Aged; Mitochondria; Muscle, Skeletal; Mutation; Myoclonus; Phenylalanine; Piracetam; Quality of Life; RNA, Transfer; Treatment Outcome; Ubiquinone; Valproic Acid	2006
Pathogenic mechanism of a human mitochondrial tRNAPhe mutation associated with myoclonic epilepsy with ragged red fibers syndrome. Proceedings of the National Academy of Sciences of the United States of America, 2007, Sep-25, Volume: 104, Issue:39 Topics: Anticodon; Base Sequence; Epilepsies, Myoclonic; Humans; Kinetics; MERRF Syndrome; Mitochondria; Molecular Conformation; Molecular Sequence Data; Mutation; Nucleic Acid Conformation; Peptide Elongation Factor Tu; Phenylalanine; RNA; RNA, Mitochondrial; RNA, Transfer, Phe	2007

Article

Year

Antimyoclonic effect of levetiracetam in MERRF syndrome.

Journal of the neurological sciences, 2006, Apr-15, Volume: 243, Issue:1-2

Topics: Activities of Daily Living; Anticonvulsants; Atrophy; Brain; Drug Therapy, Combination; Female; Genetic Predisposition to Disease; Humans; Levetiracetam; MERRF Syndrome; Middle Aged; Mitochondria; Muscle, Skeletal; Mutation; Myoclonus; Phenylalanine; Piracetam; Quality of Life; RNA, Transfer; Treatment Outcome; Ubiquinone; Valproic Acid

2006

Pathogenic mechanism of a human mitochondrial tRNAPhe mutation associated with myoclonic epilepsy with ragged red fibers syndrome.

Proceedings of the National Academy of Sciences of the United States of America, 2007, Sep-25, Volume: 104, Issue:39

Topics: Anticodon; Base Sequence; Epilepsies, Myoclonic; Humans; Kinetics; MERRF Syndrome; Mitochondria; Molecular Conformation; Molecular Sequence Data; Mutation; Nucleic Acid Conformation; Peptide Elongation Factor Tu; Phenylalanine; RNA; RNA, Mitochondrial; RNA, Transfer, Phe

2007